Safety And Tolerability Study Of RN6G In Patients With Dry, Age-Related Macular Degeneration

PHASE1CompletedINTERVENTIONAL
Enrollment

57

Participants

Timeline

Start Date

April 30, 2009

Primary Completion Date

July 31, 2011

Study Completion Date

July 31, 2011

Conditions
Age-Related MaculopathyAge-Related MaculopathiesEye DiseasesRetinal DegenerationMacular Degeneration
Interventions
BIOLOGICAL

RN6G

intravenous, single dose, dose ranging from 0.3mg/kg up to a maximum of 40 mg/kg.

BIOLOGICAL

Placebo

intravenous, single dose with experimental dose.

Trial Locations (20)

49007

Jasper Clinic, Inc., Kalamazoo

49048

Jonathan Rowe, MD, Kalamazoo

Ronald VanderLugt, MD, Kalamazoo

78217

CEDRA Clinical Research, LLC, San Antonio

Village Drive Imaging Center, San Antonio

78229

Specialty MRI, San Antonio

78233

Medical Center Ophthalmology Associates, San Antonio

78240

Medical Center Ophthalmology Associates, San Antonio

Retinal Consultants of San Antonio, San Antonio

84010

EZ Pass Rx, Bountiful

84106

Lifetree Clinical Research, Salt Lake City

84107

Rocky Mountain Eye Care Associates, LC, Salt Lake City

84124

Western Neurological Associates, Salt Lake City

85013

Dedicated Phase 1, Phoenix

85014

Retinal Consultants of AZ, Phoenix

85015

Insight Diagnostic Imaging Center, Phoenix

90301

United Medical Imaging, Inglewood

United Medical Research Institute, Inglewood

91206

Amir Hedayati-Rad, MD, Glendale

92660

California Pharmacy and Compounding Center, Newport Beach

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY